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首页> 外文期刊>Materials science & engineering >Synthesis, Characterization And In Vitro Bioactivity Of Sol-gel-derived Sio_2-cao-p_2o_5-mgo Bioglass
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Synthesis, Characterization And In Vitro Bioactivity Of Sol-gel-derived Sio_2-cao-p_2o_5-mgo Bioglass

机译:溶胶凝胶衍生的Sio_2-cao-p_2o_5-mgo生物玻璃的合成,表征和体外生物活性

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摘要

In this study, the synthesis of SiO_2-CaO-P_2O_5-MgO bioactive glass was performed by the sol-gel method. Sol-gel-derived bioglass material was produced both in powder and in discs form by uniaxial pressing, followed by sintering at 700℃. The obtained material was evaluated by X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), thermal gravimetric analysis (TGA) and differential scanning caloremetry (DSC) analyses. The biocompatibility evaluation of the formed glass was assessed through in vitro cell culture [alkaline phosphatase (AP) activity of osteoblasts] experiments and immersion studies in simulated body fluid (SBF) for different time intervals while monitoring the pH changes and the concentration of calcium, phosphorus and magnesium in the SBF medium. The SEM, XRD and FTIR studies were conducted before and after soaking of the material in SBF. At first, an amorphous calcium phosphate was formed; after 7 days this surface consisted of deposited crystalline apatite. The present investigation also revealed that the sol-gel derived quaternary bioglass system has the ability to support the growth of human fetal osteoblastic cells (hFOB 1.19). Finally, this material proved to be non-toxic and compatible for the proposed work in segmental defects in the goat model in vivo.
机译:本研究采用溶胶-凝胶法合成了SiO_2-CaO-P_2O_5-MgO生物活性玻璃。溶胶-凝胶衍生的生物玻璃材料通过单轴压制以粉末和圆盘形式生产,然后在700℃下烧结。通过X射线粉末衍射(XRD),傅里叶变换红外光谱(FTIR),扫描电子显微镜(SEM),热重分析(TGA)和差示扫描量热法(DSC)分析来评价所获得的材料。通过体外细胞培养[成骨细胞的碱性磷酸酶(AP)活性]实验和在不同时间间隔内在模拟体液(SBF)中的浸入研究,同时监测pH值变化和钙的浓度,来评估成型玻璃的生物相容性。 SBF培养基中的磷和镁。在将材料浸入SBF之前和之后进行SEM,XRD和FTIR研究。首先,形成无定形磷酸钙; 7天后,该表面由沉积的结晶磷灰石组成。本研究还揭示了溶胶-凝胶衍生的四级生物玻璃系统具有支持人类胎儿成骨细胞生长的能力(hFOB 1.19)。最终,这种材料被证明是无毒的,并且与山羊模型体内节段性缺陷的拟议工作兼容。

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